(Q2823332)
English
3-methylglutaconic aciduria type 3
3-methylglutaconic aciduria that has material basis in mutation in the OPA3 gene
- Costeff syndrome
- MGA3
- Iraqi-Jewish optic atrophy plus
- Costeff optic atrophy syndrome
- infantile optic atrophy with chorea and spastic paraplegia
- autosomal recessive optic atrophy plus syndrome
- autosomal recessive optic atrophy type 3
- 3-methylglutaconic aciduria type III
- Opa3, Autosomal Recessive
- Optic Atrophy Plus Syndrome
- MGCA3
- Iraqi-Jewish 'Optic Atrophy Plus'
- Optic Atrophy 3, Autosomal Recessive
- Optic Atrophy, Infantile, With Chorea and Spastic Paraplegia
- 3-METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3
- Mga, Type 3
- 3-METHYLGLUTACONIC ACIDURIA, TYPE III
Statements
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Identifiers
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Sitelinks
Wikipedia(7 entries)
- arwiki متلازمة كوستيف
- dewiki Costeff-Syndrom
- enwiki Costeff syndrome
- eswiki Síndrome de Costeff
- frwiki Acidurie 3-méthylglutaconique type 3
- itwiki Sindrome di Costeff
- plwiki Zespół Costeffa